4-(Diethylcarbamoyl)phenylboronic Acid
≥95%
Reagent
Code: #90527
CAS Number
389621-80-1
blur_circular Chemical Specifications
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Molecular Information
Weight
221.06 g/mol
Formula
C₁₁H₁₆BNO₃
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Registry Numbers
MDL Number
MFCD03411949
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Storage & Handling
Storage
room temperature, dry
description Product Description
Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and bioactive compounds. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds, which is crucial in drug discovery and development. Additionally, it is employed in the synthesis of boron-containing molecules for potential use in cancer therapy and as enzyme inhibitors. Its boronic acid group makes it valuable in sensing applications, particularly for detecting and quantifying sugars and other diol-containing molecules.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | White to almost white powder to crystal |
Purity | 94.5-100 |
Infrared Spectrum | Conforms to Structure |
NMR | Conforms to Structure |
shopping_cart Available Sizes & Pricing
4-(Diethylcarbamoyl)phenylboronic Acid
Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and bioactive compounds. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds, which is crucial in drug discovery and development. Additionally, it is employed in the synthesis of boron-containing molecules for potential use in cancer therapy and as enzyme inhibitors. Its boronic acid group makes it valuable in sensing applications, particularly for detecting and quantifying sugars and other diol-containing molecules.
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